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ベイズ型コピー数変異解析×コピー数変異解析×
分野バイオインフォマティクスバイオインフォマティクス
系統Process / pipelineProcess / pipeline
提唱年2004–20071998–2006
提唱者Colella et al. (QuantiSNP); Fridlyand et al. (HMM-based Bayesian CNV)Pinkel et al. (array CGH); Redon et al. (genome-wide CNV map)
種類Probabilistic genomic analysis pipelineGenomic structural variant detection pipeline
原典Colella, S., Yau, C., Taylor, J. M., Mirza, G., Butler, H., Clouston, P., Bassett, A. S., Seller, A., Holmes, C. C., & Ragoussis, J. (2007). QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Research, 35(6), 2013–2025. DOI ↗Redon, R., Ishikawa, S., Fitch, K. R., et al. (2006). Global variation in copy number in the human genome. Nature, 444(7118), 444–454. DOI ↗
別名Bayesian CNV analysis, Bayesian CNV calling, probabilistic CNV detection, Bayesian HMM-CNVCNV analysis, copy number variant detection, CNV calling, somatic copy number alteration analysis
関連66
概要Bayesian copy number variation (CNV) analysis is a probabilistic framework for detecting genomic segments where an individual's DNA copy count deviates from the diploid norm. By placing prior distributions over copy-number states and updating them with array CGH, SNP array, or sequencing read-depth evidence, the approach yields posterior probabilities for each copy-number state along the genome, providing statistically principled uncertainty quantification that frequentist segmentation methods lack.Copy number variation (CNV) analysis is a genomic pipeline for detecting regions where individuals carry fewer or more copies of a DNA segment than the reference genome. CNVs span kilobases to megabases and are a major class of structural variation implicated in cancer, neurodevelopmental disorders, and population diversity. The pipeline typically processes SNP array intensities or read-depth signals from whole-genome sequencing, applies segmentation algorithms, calls gain and loss events, and annotates them against gene and clinical databases.
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ScholarGate手法を比較: Bayesian Copy Number Variation Analysis · Copy Number Variation Analysis. 2026-06-18に以下より取得 https://scholargate.app/ja/compare